Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Quality Assurance Officer. The candidate will be responsible for implementing the Quality Management Systems at the shop floor and to ensure that Change requests, Deviation & Failure Investigations, Product Complaints, Quality Risks and CAPA are efficiently & timely managed as per the cGMP requirements.

Log in, investigate and close all event and deviations within allocated timelines as per approved procedure and issue the final report after getting signed off.
Log in, review the proposed change requests, get evaluated from relevant stake holders, and monitor the progress on implementation and close them as per approved procedure.
Log in, review the identified potential risks, evaluate and assess them for criticality and suggest mitigation plan get authorized it, monitor the implementation of action plan and close as per approved procedure.
Log in, define action items, responsibilities and timelines, get approved and close all initiated CAPA on approved format and in accordance with the approved procedure.
Log in, investigate and close all reported product technical complaints on approved format, in accordance with the approved procedure.
Maintenance and retention of all records related to Quality Systems.
To participate in the internal audit of the facility in the capacity of lead or assist auditor.
Develop and report the monthly KPIs of event & deviation, Change control, CAPA and product technical complaint on monthly basis.